Distributions of 11‐loci HLA alleles typed by amplicon‐based next‐generation sequencing in South Koreans

Abstract

The range of HLA typing for successful hematopoietic stem cell transplantation (HSCT) is gradually expanding with the next‐generation sequencing (NGS)‐based improvement in its quality. However, it is influenced by the allocation of finances and laboratory conditions. HLA‐A, ‐B, ‐C, ‐DRB1/3/4/5, ‐DQA1, ‐DQB1, ‐DPA1, and ‐DPB1 alleles were genotyped at the 3‐field level by amplicon‐based NGS using MiSeqDx system and compared to our previous study employing long‐range PCR and NGS using TruSight HLA v2 kit, in healthy donors from South Korea. Exon 2, exons 2/3, exons 2/3/4 or 5 of 11‐loci were amplified by multiplex PCR. The sequence reads of over 53 depth counts were consistently obtained in each sample exon, depending on the target exon determined to match the reference sequence contained in the IPD‐IMGT/HLA Database. HLA alleles were investigated by combinations of the determined exons. A total of 18 alleles with a frequency over 10% were found at the 11 HLA loci. Three ambiguities of HLA‐A, ‐C, and ‐DRB1 were resolved. We observed a total of 26 HLA‐A ~ C ~ B and 6 HLA‐DRB1 ~ DQA1 ~ DQB1 ~ DPA1 ~ DPB1 haplotypes having significant linkage disequilibrium between alleles at all neighboring HLA loci. This result was compatible with the previous one, using TruSight HLA v2 kit. Advantages are simple and short progress time because one plate is used for each PCR step in one PCR machine and 11‐loci HLA typing is possible even if only eight samples. These data suggested that expanded 11‐loci HLA typing data by amplicon‐based NGS might help perform HSCT.